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Association of Lipoprotein-Associated Phospholipase A2 with the Prevalence of Nonalcoholic Fatty Liver Disease: A Result from the APAC Study

Nonalcoholic fatty liver disease (NAFLD) is a worldwide chronic liver disease. Few studies have investigated the association between NAFLD and Lipoprotein-associated phospholipase A(2) (Lp-PLA(2)), a unique enzyme correlated with oxidative stress. The aim of this study was to assess the relationship...

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Autores principales: Liu, Zhongni, Li, Hong, Zheng, Yinghong, Gao, Ziyu, Cong, Lin, Yang, Liming, Zhou, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031645/
https://www.ncbi.nlm.nih.gov/pubmed/29973631
http://dx.doi.org/10.1038/s41598-018-28494-8
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author Liu, Zhongni
Li, Hong
Zheng, Yinghong
Gao, Ziyu
Cong, Lin
Yang, Liming
Zhou, Yong
author_facet Liu, Zhongni
Li, Hong
Zheng, Yinghong
Gao, Ziyu
Cong, Lin
Yang, Liming
Zhou, Yong
author_sort Liu, Zhongni
collection PubMed
description Nonalcoholic fatty liver disease (NAFLD) is a worldwide chronic liver disease. Few studies have investigated the association between NAFLD and Lipoprotein-associated phospholipase A(2) (Lp-PLA(2)), a unique enzyme correlated with oxidative stress. The aim of this study was to assess the relationship between Lp-PLA(2) and NAFLD in a Chinese community-based cohort. A total of 1587 adults aged ≥40 years were enrolled in the current study. Participants underwent a standardized evaluation. The serum Lp-PLA2 concentration was measured by ELISA and NAFLD was diagnosed by ultrasonography. Multivariable logistic regression was used to assess the association between Lp-PLA2 and NAFLD. Increased Lp-PLA2 levels were significantly associated with decreased NAFLD prevalence after adjusting for other potential confounders. The adjusted ORs of NAFLD in Q2, Q3 and Q4 compared with Q1 were 0.88 (0.64–1.21), 0.71 (0.51–0.98) and 0.67 (0.48–0.95), respectively (P < 0.05). Furthermore, the adjusted ORs of moderate and heavy NAFLD in Q2, Q3 and Q4 compared to Q1 were 0.64 (0.41–1.01), 0.48 (0.29–0.80) and 0.47 (0.28–0.79), respectively (P < 0.01). In conclusions, increased Lp-PLA2 levels were independently associated with decreased NAFLD prevalence.
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spelling pubmed-60316452018-07-12 Association of Lipoprotein-Associated Phospholipase A2 with the Prevalence of Nonalcoholic Fatty Liver Disease: A Result from the APAC Study Liu, Zhongni Li, Hong Zheng, Yinghong Gao, Ziyu Cong, Lin Yang, Liming Zhou, Yong Sci Rep Article Nonalcoholic fatty liver disease (NAFLD) is a worldwide chronic liver disease. Few studies have investigated the association between NAFLD and Lipoprotein-associated phospholipase A(2) (Lp-PLA(2)), a unique enzyme correlated with oxidative stress. The aim of this study was to assess the relationship between Lp-PLA(2) and NAFLD in a Chinese community-based cohort. A total of 1587 adults aged ≥40 years were enrolled in the current study. Participants underwent a standardized evaluation. The serum Lp-PLA2 concentration was measured by ELISA and NAFLD was diagnosed by ultrasonography. Multivariable logistic regression was used to assess the association between Lp-PLA2 and NAFLD. Increased Lp-PLA2 levels were significantly associated with decreased NAFLD prevalence after adjusting for other potential confounders. The adjusted ORs of NAFLD in Q2, Q3 and Q4 compared with Q1 were 0.88 (0.64–1.21), 0.71 (0.51–0.98) and 0.67 (0.48–0.95), respectively (P < 0.05). Furthermore, the adjusted ORs of moderate and heavy NAFLD in Q2, Q3 and Q4 compared to Q1 were 0.64 (0.41–1.01), 0.48 (0.29–0.80) and 0.47 (0.28–0.79), respectively (P < 0.01). In conclusions, increased Lp-PLA2 levels were independently associated with decreased NAFLD prevalence. Nature Publishing Group UK 2018-07-04 /pmc/articles/PMC6031645/ /pubmed/29973631 http://dx.doi.org/10.1038/s41598-018-28494-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liu, Zhongni
Li, Hong
Zheng, Yinghong
Gao, Ziyu
Cong, Lin
Yang, Liming
Zhou, Yong
Association of Lipoprotein-Associated Phospholipase A2 with the Prevalence of Nonalcoholic Fatty Liver Disease: A Result from the APAC Study
title Association of Lipoprotein-Associated Phospholipase A2 with the Prevalence of Nonalcoholic Fatty Liver Disease: A Result from the APAC Study
title_full Association of Lipoprotein-Associated Phospholipase A2 with the Prevalence of Nonalcoholic Fatty Liver Disease: A Result from the APAC Study
title_fullStr Association of Lipoprotein-Associated Phospholipase A2 with the Prevalence of Nonalcoholic Fatty Liver Disease: A Result from the APAC Study
title_full_unstemmed Association of Lipoprotein-Associated Phospholipase A2 with the Prevalence of Nonalcoholic Fatty Liver Disease: A Result from the APAC Study
title_short Association of Lipoprotein-Associated Phospholipase A2 with the Prevalence of Nonalcoholic Fatty Liver Disease: A Result from the APAC Study
title_sort association of lipoprotein-associated phospholipase a2 with the prevalence of nonalcoholic fatty liver disease: a result from the apac study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031645/
https://www.ncbi.nlm.nih.gov/pubmed/29973631
http://dx.doi.org/10.1038/s41598-018-28494-8
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